Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07234292

Evaluation of Patient Satisfaction With Blephaderm as a Complementary Care in Post-eyelid Surgery.

Evaluation of Patient Satisfaction With a New Preservative-free Eyelid Cream as a Complementary Care in Post-eyelid Surgery: The ADMIRE Study

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
30 (estimated)
Sponsor
Laboratoires Thea · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this non-interventional, open and monocentric study is to evaluate the satisfaction of 30 patients, after 3 months with Blephaderm eyelid cream, as a complementary care in post-eyelid surgery (Blepharopasty or ptosis). The participant will be asked to use Blephaderm twice a day. The patient satisfaction will be evaluated using a VAS scale.

Conditions

Interventions

TypeNameDescription
OTHERCosmetic: BlephadermPreservative free eyelid cream: Aqua (water), oleyl erucate, trehalose, sodium acrylates copolymer, lecithin, Ophiopogon japonicus root extract, hydrolyzed hyaluronic acid, maltodextrin, tocopherol, sodium hydroxide, phytic acid, Glycine soja (soybean) oil, Helianthus annuus seed oil.

Timeline

Start date
2025-11-15
Primary completion
2026-05-15
Completion
2026-05-15
First posted
2025-11-18
Last updated
2025-11-18

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT07234292. Inclusion in this directory is not an endorsement.